We found 14 genetics specialists near Dayton, OH.

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Specializes in Genetics
3700 Southern Boulevard; Suite 401
Kettering, OH
 

Ms. Meghan Lundy practices genetics in Kettering, OH. Ms. Lundy is professionally affiliated with Kettering Health Network.

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Specializes in Pediatrics, Genetics
One Childrens Plaza
Dayton, OH
 

Dr. Marvin Miller practices genetics. Dr. Miller attended medical school at Yale School of Medicine. He takes several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic.

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Specializes in General Practice, Clinical Biochemical Genetics
1 Childrens Plaza
Dayton, OH
 

Dr. John Karl De Dios' areas of specialization are general practice and clinical biochemical genetics. He honors Humana HMO, Humana Bronze, Humana Catastrophic, and more.

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Specializes in Genetics
1 Childrens Plaza
Dayton, OH
 

Specializes in Genetics
1269 Colfax Avenue
Kettering, OH
 

Ms. Julie Edsall works as a genetics specialist. She is in-network for several insurance carriers, including Humana HMO, Humana Bronze, and Humana Catastrophic.

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Specializes in Genetics
1 Wyoming Street; Berry Pavilion
Dayton, OH
 

Specializes in Genetics
1 Childrens Plaza
Dayton, OH
 

Specializes in Genetics
1 Childrens Plaza
Dayton, OH
 

Specializes in Genetics
1 Wyoming Street
Dayton, OH
 

Specializes in Genetics
1 Childrens Plaza
Dayton, OH
 

Specializes in Genetics
1 Childrens Plaza
Dayton, OH
 

Specializes in Genetics
4100 W 3rd Street
Dayton, OH
 

Specializes in Genetics
1 Wyoming Street; Mvh - Berry Building
Dayton, OH
 

Specializes in Genetics
1 Childrens Plaza
Dayton, OH
 

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What is Genetics?

Genetics is the branch of medicine dealing with the diagnosis, prevention, and treatment of genetically-linked or hereditary diseases. It includes both genetic counselors and medical geneticists, who may be involved in either patient care or research.

Medical geneticists are doctors who study genes and diseases that are caused by genes. There are many diseases linked to genetics, including:
  • Single gene disorders, the result of a single mutated gene. Examples include Huntington’s disease, which causes jerky movements, and sickle-cell anemia, where red blood cells have an abnormal, rigid shape.
  • Inborn metabolic disorders, which are a specific type of single gene disorder that results in abnormalities in the way the body chemically processes proteins, carbohydrates or fats. Some examples are Urea Cycle Disorder (where ammonia builds up in the body) and Gaucher’s Disease (where fatty substances build up in cells and organs).
  • Chromosomal disorders, where gene-carrying chromosomes do not pair up correctly or are missing. Some examples are Klinefelter Syndrome, a sex-chromosome disorder, and Down Syndrome.
  • Congenital abnormalities (commonly known as birth defects), which can be caused by genetic abnormalities. They also can happen because of illness or environmental exposure during pregnancy (such as with rubella), or for unknown reasons.
  • Other common diseases that have hereditary traits, such diabetes, autism, and some types of cancer.

Medical geneticists typically spend their career in research, although some treat or counsel patients. A patient may see a medical geneticist to obtain more information about their disorder or about how an inherited disorder might impact their family. The field of medical genetics includes the following four subspecialties:
  • Clinical Genetics: This overarching branch of medical genetics deals with the treatment and management of hereditary diseases.
  • Biomechanical Genetics: This branch deals with metabolic disorders, such as galactosemia and phenylketonuria.
  • Cytogenetics: This specialty deals with chromosomes and their associated diseases, as well as testing their structure and number.
  • Molecular Genetics: This specialty focuses on DNA, interpreting DNA sequencing and other tests, and relating DNA information to specific diseases.

Related to medical genetics is the field of genetic counseling. These healthcare professionals are not physicians, but they are educators who help patients interpret medical information about genetic risk, which can sometimes be difficult to understand or overwhelming. When families face the possibility of having a child with an inherited disease, genetic counselors educate them about their specific risks and options. They analyze patterns in family history and interpret the medical probability of a genetic disease occurring. They provide support and put families in contact with resources. Genetic counselors help families adapt to all of the implications that a hereditary disease can have in their life.
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